Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tsubasa Oguni"'
Autor:
Nivethitha Arunkumar, Dung Chi Vu, Shaukat Khan, Hironori Kobayashi, Thi Bich Ngoc Can, Tsubasa Oguni, Jun Watanabe, Misa Tanaka, Seiji Yamaguchi, Takeshi Taketani, Yasuhiko Ago, Hidenori Ohnishi, Sampurna Saikia, José V. Álvarez, Shunji Tomatsu
Publikováno v:
Diagnostics, Vol 11, Iss 8, p 1347 (2021)
Mucopolysaccharidoses (MPS) and mucolipidosis (ML II/III) are a group of lysosomal storage disorders (LSDs) that occur due to a dysfunction of the lysosomal hydrolases responsible for the catabolism of glycosaminoglycans (GAGs). However, ML is caused
Externí odkaz:
https://doaj.org/article/5b84ef58506c4633ac775936c0469044
Autor:
Tsubasa Oguni, Shunji Tomatsu, Misa Tanaka, Kenji Orii, Toshiyuki Fukao, Jun Watanabe, Seiji Fukuda, Yoshitomo Notsu, Dung Chi Vu, Thi Bich Ngoc Can, Atsushi Nagai, Seiji Yamaguchi, Takeshi Taketani, Michael H. Gelb, Hironori Kobayashi
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 6, p 2025 (2020)
Mucopolysaccharidoses (MPSs) are rare lysosomal storage diseases caused by the accumulation of undegraded glycosaminoglycans in cells and tissues. The effectiveness of early intervention for MPS has been reported. Multiple-assay formats using tandem
Externí odkaz:
https://doaj.org/article/168d95bf9c244438b04a3d1ddcb9ebba
Autor:
Jun Watanabe, Shaukat Khan, Misa Tanaka, Takeshi Taketani, Hironori Kobayashi, Seiji Yamaguchi, Hidenori Ohnishi, Thi Bich Ngoc Can, Tsubasa Oguni, Yasuhiko Ago, Nivethitha Arunkumar, Shunji Tomatsu, Dung Chi Vu, Sampurna Saikia, José V. Álvarez
Publikováno v:
Diagnostics, Vol 11, Iss 1347, p 1347 (2021)
Diagnostics
Volume 11
Issue 8
Diagnostics
Volume 11
Issue 8
Mucopolysaccharidoses (MPS) and mucolipidosis (ML II/III) are a group of lysosomal storage disorders (LSDs) that occur due to a dysfunction of the lysosomal hydrolases responsible for the catabolism of glycosaminoglycans (GAGs). However, ML is caused
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1181cc49674ccf924cebeac7162ad520
https://doi.org/10.3390/diagnostics11081347
https://doi.org/10.3390/diagnostics11081347
Autor:
Hironori Kobayashi, Shunji Tomatsu, Takeshi Taketani, Kenji E. Orii, Atsushi Nagai, Yoshitomo Notsu, Toshiyuki Fukao, Jun Watanabe, Tsubasa Oguni, Misa Tanaka, Thi Bich Ngoc Can, Michael H. Gelb, Dung Chi Vu, Seiji Yamaguchi, Seiji Fukuda
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 6
International Journal of Molecular Sciences, Vol 21, Iss 6, p 2025 (2020)
Volume 21
Issue 6
International Journal of Molecular Sciences, Vol 21, Iss 6, p 2025 (2020)
Mucopolysaccharidoses (MPSs) are rare lysosomal storage diseases caused by the accumulation of undegraded glycosaminoglycans in cells and tissues. The effectiveness of early intervention for MPS has been reported. Multiple-assay formats using tandem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93a3c9498eec675bd056e1964f65f57a
https://doi.org/10.3390/ijms21062025
https://doi.org/10.3390/ijms21062025